Homoaromaticity (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Homoaromaticity" in English language version.

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doi.org (Global: 2nd place; English: 2nd place)

  • IUPAC, Compendium of Chemical Terminology, 5th ed. (the "Gold Book") (2025). Online version: (2006–) "Homoaromatic". doi:10.1351/goldbook.H02839
  • Winstein, S (1959). "Homo-Aromatic Structures". J. Am. Chem. Soc. 81 (24): 6523. doi:10.1021/ja01533a052.
  • Freeman, P. K. (2005). "Neutral Homoaromaticity in Some Neutral Heterocycles". J. Org. Chem. 70 (6): 1998–2001. doi:10.1021/jo040250o. PMID 15760178.
  • Winstein, S.; Sonnenberg, J.; DeVries, L. (1959). "The Tris-Homocyclopropenyl Cation". J. Am. Chem. Soc. 81 (24): 6523–6524. doi:10.1021/ja01533a051.
  • Childs, R. F. (1984). "The Homotropylium Ion and Homoaromaticity". Acc. Chem. Res. 17 (10): 347–352. doi:10.1021/ar00106a001.
  • Schleyer, P. R. (2001). "Introduction: Aromaticity". Chem. Rev. 101 (5): 1115–1118. doi:10.1021/cr0103221. PMID 11749368.
  • Rosenburg, J. L.; Mahler, J. E.; Pettit, R. J. (1962). "The Bicyclo[5.1.0]octadienyl Cation, A New Stable Carbonium Ion". J. Am. Chem. Soc. 84 (14): 2842–2843. doi:10.1021/ja00873a051.
  • Winstein, S.; Kaesz, H.D.; Kreiter, C.G.; Friedrich, E.C. (1965). "Homotropylium Ion and its Molybdenum Tricarbonyl Complex". J. Am. Chem. Soc. 87 (14): 3267–3269. doi:10.1021/ja01092a060.
  • Winstein, S.; Kreiter, C.G.; Brauman, J.I. (1966). "Ring Inversion, Ultraviolet Spectrum, and Electronic Structure of the Monohomotropylium Ion". J. Am. Chem. Soc. 88 (9): 2047–2048. doi:10.1021/ja00961a037.
  • Haddon, R.C. (1975). "The structure of the homotropenylium cation". Tetrahedron Lett. 16 (11): 863–866. doi:10.1016/S0040-4039(00)72004-1.
  • Haddon, R.C. (1975). "Perturbational molecular orbital (PMO) theory of homoaromaticity". J. Am. Chem. Soc. 97 (13): 3608–3615. doi:10.1021/ja00846a009.
  • Oth, J.F.M.; Smith, D.M.; Prange, U.; Schröder, G. (1973). "A [16]Annulenediyl Dication". Angew. Chem. Int. Ed. Engl. 12 (4): 327–328. doi:10.1002/anie.197303271.
  • Sal'nikov, G.E.; Genaev, A.M.; Mamatyuk, V.I.; Shubin, V.G. (2008). "Homophenalenyl cations, new representatives of homoaromatic systems". Russ. J. Org. Chem. 44 (7): 1000–1005. doi:10.1134/S1070428008070099. S2CID 93688550.
  • Exner, Kai; Schleyer, Paul von Ragué (2001). "Theoretical Bond Energies: A Critical Evaluation". J. Phys. Chem. A. 105 (13): 3407–3416. Bibcode:2001JPCA..105.3407E. doi:10.1021/jp004193o.
  • Prinzbach, H.; Gescheidt, G.; Martin, H.-D.; Herges, R.; Heinze, J.; Prakash, G. K. Surya; Olah, G. A. "Cyclic electron delocalization in hydrocarbon cages (pagodanes, isopagodanes, (bisseco-/seco-)-(dodecahedradienes))". Pure and Applied Chemistry. 67 (5): 673–682, 1995. doi:10.1351/pac199567050673. S2CID 96232491.
  • Suzuki, T.; Li, Q.; Khemani, K.C.; Wudl, F. (1992). "Dihydrofulleroid H3C61: synthesis and properties of the parent fulleroid". J. Am. Chem. Soc. 114 (18): 7301–7302. doi:10.1021/ja00044a055.
  • Tran Ngoc, Trung; Grabicki, Niklas; Irran, Elisabeth; Dumele, Oliver; Teichert, Johannes F. (March 2023). "Photoswitching neutral homoaromatic hydrocarbons". Nature Chemistry. 15 (3): 377–385. doi:10.1038/s41557-022-01121-w. ISSN 1755-4349. PMC 9986110. PMID 36702883.
  • Tran Ngoc, Trung; van der Welle, Jasper; Rüffer, Tobias; Teichert, Johannes F. (2023-07-03). "Synthesis of Stable Neutral Homoaromatic Hydrocarbons". Synthesis. doi:10.1055/s-0042-1751468. ISSN 0039-7881.
  • Zimmerman, H. E.; Grunewald, G. L. (1966). "The Chemistry of Barrelene. III. A Unique Photoisomerization to Semibullvalene". Journal of the American Chemical Society. 88: 183–184. doi:10.1021/ja00953a045.
  • Dewar, M.J.S.; Lo, D.H. (1971). "Ground states of .sigma.-bonded molecules. XIV. Application of energy partitioning to the MINDO/2 method and a study of the Cope rearrangement". J. Am. Chem. Soc. 93 (26): 7201–7207. doi:10.1021/ja00755a014.
  • Hoffman, D.; Stohrer, W-D (1971). "Cope rearrangement revisited". J. Am. Chem. Soc. 93 (25): 6941–6948. doi:10.1021/ja00754a042.
  • Griffiths, P. R.; Pivonka, D. E.; Williams, R. V. (2011). "The Experimental Realization of a Neutral Homoaromatic Carbocycle". Chemistry: A European Journal. 17 (33): 9193–9199. doi:10.1002/chem.201100025. PMID 21735493.
  • Steiner, D.; Balzereit, C.; Winkler, H. J. R.; Stamatis, N.; Massa, W.; Berndt, A.; Hofmann, M.; Von Ragué Schleyer, P. (1994). "Nonclassical 1,2-Diboretanes and 1,2-Diborolanes". Angewandte Chemie International Edition in English. 33 (22): 2303–2306. doi:10.1002/anie.199423031.
  • Martin, H.D.; Mayer, B. (1983). "Proximity Effects in Organic Chemistry?The Photoelectron Spectroscopic Investigation of Non-Bonding and Transannular Interactions". Angew. Chem. Int. Ed. Engl. 22 (4): 283–314. doi:10.1002/anie.198302831.
  • Steiner, D.; Winkler, H.; Balzereit, C.; Happel, T.; Hofmann, M.; Subramanian, G.; Schleyer, P.V.R.; Massa, W.; Berndt, A. (1996). "1,2-Diboretanides: Homoaromatic 2π-Electron Compounds with High Inversion Barriers". Angew. Chem. Int. Ed. Engl. 35 (17): 1990–1992. doi:10.1002/anie.199619901.
  • Exner, K.; Hunkler, D.; Gescheidt, G.; Prinzbach, H. (1998). "Do Nonclassical, Cyclically Delocalized 4N/5e Radical Anions and 4N/6e Dianions Exist? – One- and Two-Electron Reduction of Proximate, Synperiplanar Bis-Diazenes". Angew. Chem. Int. Ed. Engl. 37 (13–14): 1910–1913. doi:10.1002/(SICI)1521-3773(19980803)37:13/14<1910::AID-ANIE1910>3.0.CO;2-D.
  • Exner, K.; Cullmann, O.; Vögtle, M.; Prinzbach, H.; Grossmann, B.; Heinze, J.; Liesum, L.; Bachmann, R.; Schweiger, A.; Gescheidt, G. (2000). "Cyclic In-Plane Electron Delocalization (σ-Bishomoaromaticity) in 4N/5e Radical Anions and 4N/6e Dianions – Generation, Structures, Properties, Ion-Pairing, and Calculations". J. Am. Chem. Soc. 122 (43): 10650–10660. doi:10.1021/ja0014943.
  • Volz, H.; Shin, J. (2006). "Bicyclo[3.2.1]octa-3,6-dien-2-yl Cation: A Bishomoantiaromate". J. Org. Chem. 71 (6): 2220–2226. doi:10.1021/jo0515125. PMID 16526766.

harvard.edu (Global: 18th place; English: 17th place)

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iupac.org (Global: 538th place; English: 863rd place)

goldbook.iupac.org

  • IUPAC, Compendium of Chemical Terminology, 5th ed. (the "Gold Book") (2025). Online version: (2006–) "Homoaromatic". doi:10.1351/goldbook.H02839

nature.com (Global: 234th place; English: 397th place)

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semanticscholar.org (Global: 11th place; English: 8th place)

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